Direct access to functionalized azepanes by cross-coupling with α-halo eneformamides

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Abstract

The synthesis of functionalized azepanes was accomplished through the palladium-mediated cross-coupling of α-halo eneformamides with mostly unactivated nucleophiles under mild conditions. Alkenylations proceeded with excellent stereoselectivitiy. In most cases, high yields of the coupling products were obtained. © 2014 American Chemical Society.

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Beng, T. K., Wilkerson-Hill, S. M., & Sarpong, R. (2014). Direct access to functionalized azepanes by cross-coupling with α-halo eneformamides. Organic Letters, 16(3), 916–919. https://doi.org/10.1021/ol403671s

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